Canonical Allele Identifier: CA1768019971

Gene: ASAH1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18061425A= , CM000670.2:g.18061425A=	GRCh38
NC_000008.10:g.17918934A= , CM000670.1:g.17918934A=	GRCh37
NC_000008.9:g.17963214A=	NCBI36
NG_008985.1:g.28574T=
NG_008985.2:g.28574T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381733.9:c.785T=	ENSP00000371152.4:p.Val262=
ENST00000517409.2:n.705T=
ENST00000518746.2:n.2423T=
ENST00000519545.6:n.754T=
ENST00000520781.6:c.662T=	ENSP00000427751.1:p.Val221=
ENST00000521542.2:n.45T=
ENST00000635756.1:c.150T=
ENST00000635944.1:c.*573T=	ENSP00000490195.1:n.*573T=
ENST00000635998.1:c.737T=	ENSP00000490506.1:p.Val246=
ENST00000636009.1:c.594T=	ENSP00000489988.1:n.594T=
ENST00000636033.1:c.*573T=	ENSP00000489617.1:n.*573T=
ENST00000636050.1:c.*580T=	ENSP00000490562.1:n.*580T=
ENST00000636128.1:c.416T=	ENSP00000489789.1:p.Val139=
ENST00000636160.1:c.*629T=	ENSP00000489651.1:n.*629T=
ENST00000636171.1:c.680T=	ENSP00000489761.1:p.Val227=
ENST00000636455.1:c.785T=	ENSP00000490502.1:p.Val262=
ENST00000636494.1:c.*517T=	ENSP00000490388.1:n.*517T=
ENST00000636563.1:n.399T=
ENST00000636577.1:c.677T=	ENSP00000490027.1:p.Val226=
ENST00000636691.1:c.542T=	ENSP00000490725.1:p.Val181=
ENST00000636701.1:c.*388T=	ENSP00000489800.1:n.*388T=
ENST00000636815.1:c.654T=
ENST00000636920.1:c.*573T=	ENSP00000490437.1:n.*573T=
ENST00000636997.1:c.650T=	ENSP00000490093.1:p.Val217=
ENST00000637013.1:c.*1105T=	ENSP00000490596.1:n.*1105T=
ENST00000637014.1:n.1144T=
ENST00000637095.1:c.*517T=	ENSP00000490415.1:n.*517T=
ENST00000637244.1:c.*1255T=	ENSP00000490188.1:n.*1255T=
ENST00000637343.1:n.2174T=
ENST00000637429.1:c.*949T=	ENSP00000490522.1:n.*949T=
ENST00000637484.1:c.*699T=	ENSP00000490837.1:n.*699T=
ENST00000637528.1:c.674T=	ENSP00000490801.1:p.Val225=
ENST00000637609.1:n.3458T=
ENST00000637636.1:c.731T=	ENSP00000490112.1:p.Val244=
ENST00000637790.2:c.737T= MANE Select	ENSP00000490272.1:p.Val246=
ENST00000637857.1:n.1103T=
ENST00000637922.1:c.542T=	ENSP00000490071.1:p.Val181=
ENST00000637991.1:c.710T=	ENSP00000489901.1:p.Val237=
ENST00000638028.1:n.954T=
ENST00000638069.1:n.1558T=
ENST00000262097.10:c.737T=	ENSP00000262097.6:p.Val246=
ENST00000314146.10:c.719T=	ENSP00000326970.10:p.Val240=
ENST00000381733.8:c.785T=	ENSP00000371152.4:p.Val262=
ENST00000518746.1:n.554T=
ENST00000519468.5:n.566T=
ENST00000520781.5:c.662T=	ENSP00000427751.1:p.Val221=
ENST00000521542.1:n.450T=
NM_001127505.1:c.719T=	NP_001120977.1:p.Val240=
NM_001127505.2:c.719T=	NP_001120977.1:p.Val240=
NM_004315.4:c.785T=	NP_004306.3:p.Val262=
NM_004315.5:c.785T=	NP_004306.3:p.Val262=
NM_177924.3:c.737T=	NP_808592.2:p.Val246=
NM_177924.4:c.737T=	NP_808592.2:p.Val246=
XM_005273504.2:c.671T=	XP_005273561.1:p.Val224=
NM_001363743.1:c.542T=	NP_001350672.1:p.Val181=
XM_005273504.3:c.671T=	XP_005273561.1:p.Val224=
NM_177924.5:c.737T= MANE Select	NP_808592.2:p.Val246=
NM_001127505.3:c.719T=	NP_001120977.1:p.Val240=
NM_001363743.2:c.542T=	NP_001350672.1:p.Val181=
NM_004315.6:c.785T=	NP_004306.3:p.Val262=